geneid | 284996 |
---|---|
ensemblid | ENSG00000163162.9 |
hgncid | 23137 |
symbol | RNF149 |
name | ring finger protein 149 |
refseq_nuc | NM_173647.4 |
refseq_prot | NP_775918.2 |
ensembl_nuc | ENST00000295317.4 |
ensembl_prot | ENSP00000295317.3 |
mane_status | MANE Select |
chr | chr2 |
start | 101275601 |
end | 101308701 |
strand | - |
ver | v1.2 |
region | chr2:101275601-101308701 |
region5000 | chr2:101270601-101313701 |
regionname0 | RNF149_chr2_101275601_101308701 |
regionname5000 | RNF149_chr2_101270601_101313701 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 400 | 181 | 18 | 31 | 94 | 13 | 25 | 74 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0002 | 0/0 | 400 | 139 | 39 | 23 | 63 | 2 | 12 | 54 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0003 | 0/1 | 400 | 46 | 30 | 8 | 0 | 1 | 6 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0004 | 0/0 | 400 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0005 | 0/0 | 400 | 3 | 0 | 2 | 1 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0006 | 0/0 | 400 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0007 | 0/0 | 400 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0008 | 0/0 | 400 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0009 | 1/0 | 400 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0010 | 0/0 | 400 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1203 | 181 | 18 | 31 | 94 | 13 | 25 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
c0002 | 0/0 | 1203 | 139 | 39 | 23 | 63 | 2 | 12 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
c0003 | 0/1 | 1203 | 46 | 30 | 8 | 0 | 1 | 6 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
c0004 | 0/0 | 1203 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
c0005 | 0/0 | 1203 | 3 | 0 | 2 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
c0006 | 1/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
c0007 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
c0008 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
c0009 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
c0010 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1751 | 160 | 30 | 25 | 78 | 6 | 21 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0002 | 0/0 | 1751 | 134 | 19 | 29 | 70 | 6 | 10 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0003 | 1/1 | 1751 | 62 | 30 | 10 | 9 | 1 | 10 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0004 | 0/0 | 1748 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0005 | 0/0 | 1751 | 3 | 0 | 0 | 0 | 3 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0006 | 0/0 | 1751 | 3 | 3 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0007 | 0/0 | 1751 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0008 | 0/0 | 1751 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0009 | 0/0 | 1751 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0010 | 0/0 | 1751 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0011 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0012 | 0/0 | 1751 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0013 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0014 | 0/0 | 1609 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0015 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0016 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
t0017 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 22 | 0 | 6 | 14 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0002 | 0/0 | 21 | 2 | 4 | 11 | 2 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0003 | 0/0 | 13 | 4 | 0 | 9 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0004 | 0/0 | 9 | 0 | 5 | 4 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0014 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0018 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0038 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1203 | 181 | 18 | 31 | 94 | 13 | 25 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0002c0002 | 0/0 | 1203 | 139 | 39 | 23 | 63 | 2 | 12 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0003c0003 | 0/1 | 1203 | 46 | 30 | 8 | 0 | 1 | 6 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0004c0004 | 0/0 | 1203 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0005c0005 | 0/0 | 1203 | 3 | 0 | 2 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0006c0010 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0007c0008 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0008c0009 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0009c0006 | 1/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0010c0007 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2953 | 45 | 0 | 4 | 24 | 4 | 13 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0001c0001t0002 | 0/0 | 2953 | 129 | 18 | 27 | 68 | 6 | 10 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0001c0001t0005 | 0/0 | 2953 | 3 | 0 | 0 | 0 | 3 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0001c0001t0007 | 0/0 | 2953 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0001c0001t0009 | 0/0 | 2953 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0001c0001t0010 | 0/0 | 2953 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0002c0002t0001 | 0/0 | 2953 | 112 | 29 | 21 | 53 | 2 | 7 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0002c0002t0002 | 0/0 | 2953 | 2 | 1 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0002c0002t0003 | 0/0 | 2953 | 19 | 5 | 2 | 8 | 0 | 4 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0002c0002t0008 | 0/0 | 2953 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0002c0002t0011 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0002c0002t0012 | 0/0 | 2953 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0002c0002t0014 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0002c0002t0015 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0002c0002t0016 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0003c0003t0003 | 0/1 | 2953 | 41 | 25 | 8 | 0 | 1 | 6 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0003c0003t0006 | 0/0 | 2953 | 3 | 3 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0003c0003t0013 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0003c0003t0017 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0004c0004t0004 | 0/0 | 2950 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0005c0005t0002 | 0/0 | 2953 | 3 | 0 | 2 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0006c0010t0001 | 0/0 | 2953 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0007c0008t0001 | 0/0 | 2953 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0008c0009t0003 | 0/0 | 2953 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0009c0006t0003 | 1/0 | 2953 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
a0010c0007t0001 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | copy fasta | chr2 | 101270601 | 101313701 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0001 | 0/0 | 22 | 0 | 6 | 14 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0004 | 0/0 | 9 | 0 | 5 | 4 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0014 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0018 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0005g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0001c0001t0010g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0002 | 0/0 | 21 | 2 | 4 | 11 | 2 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0003 | 0/0 | 13 | 4 | 0 | 9 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0008g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0012g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0014g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0015g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0002c0002t0016g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0038 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0013g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0003c0003t0017g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0004c0004t0004g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0005c0005t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0005c0005t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0005c0005t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0006c0010t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0007c0008t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0008c0009t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0009c0006t0003g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
a0010c0007t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0031 | EUR | GBR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0073 | EUR | GBR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0052 | EUR | GBR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | FIN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | FIN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0080 | EUR | FIN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00621 | hp2 | a0001 | c0001 | t0007 | g0050 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00642 | hp2 | a0003 | c0003 | t0003 | g0021 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0174 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01074 | hp2 | a0003 | c0003 | t0003 | g0021 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01099 | hp2 | a0003 | c0003 | t0003 | g0187 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01167 | hp1 | a0005 | c0005 | t0002 | g0114 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01167 | hp2 | a0003 | c0003 | t0003 | g0177 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01169 | hp1 | a0005 | c0005 | t0002 | g0095 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01175 | hp2 | a0003 | c0003 | t0003 | g0166 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01243 | hp1 | a0002 | c0002 | t0003 | g0046 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01255 | hp1 | a0003 | c0003 | t0003 | g0178 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01346 | hp2 | a0003 | c0003 | t0003 | g0186 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01358 | hp1 | a0002 | c0002 | t0003 | g0229 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0217 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01361 | hp2 | a0003 | c0003 | t0003 | g0179 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0081 | EUR | IBS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0146 | EUR | IBS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0031 | EUR | IBS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02040 | hp1 | a0007 | c0008 | t0001 | g0153 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02071 | hp1 | a0001 | c0001 | t0007 | g0049 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02080 | hp1 | a0002 | c0002 | t0003 | g0041 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02145 | hp1 | a0003 | c0003 | t0003 | g0008 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02145 | hp2 | a0002 | c0002 | t0015 | g0161 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0165 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02258 | hp2 | a0004 | c0004 | t0004 | g0013 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0159 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0175 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02451 | hp2 | a0003 | c0003 | t0003 | g0160 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02572 | hp1 | a0003 | c0003 | t0003 | g0170 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02572 | hp2 | a0002 | c0002 | t0003 | g0227 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02602 | hp1 | a0006 | c0010 | t0001 | g0235 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02615 | hp1 | a0010 | c0007 | t0001 | g0148 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02615 | hp2 | a0003 | c0003 | t0003 | g0180 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02622 | hp1 | a0003 | c0003 | t0003 | g0168 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02647 | hp2 | a0003 | c0003 | t0003 | g0008 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02683 | hp2 | a0003 | c0003 | t0003 | g0035 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02698 | hp2 | a0003 | c0003 | t0003 | g0047 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02717 | hp1 | a0003 | c0003 | t0003 | g0154 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02723 | hp1 | a0003 | c0003 | t0006 | g0191 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02723 | hp2 | a0003 | c0003 | t0003 | g0036 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02809 | hp2 | a0003 | c0003 | t0003 | g0022 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0216 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02818 | hp2 | a0003 | c0003 | t0017 | g0236 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02886 | hp1 | a0003 | c0003 | t0003 | g0008 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02895 | hp1 | a0003 | c0003 | t0003 | g0169 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02896 | hp1 | a0003 | c0003 | t0003 | g0022 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02897 | hp1 | a0003 | c0003 | t0003 | g0022 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02965 | hp2 | a0003 | c0003 | t0013 | g0183 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0218 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03017 | hp1 | a0003 | c0003 | t0003 | g0230 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03017 | hp2 | a0003 | c0003 | t0003 | g0038 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03041 | hp1 | a0003 | c0003 | t0006 | g0190 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0199 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03130 | hp1 | a0002 | c0002 | t0003 | g0040 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03130 | hp2 | a0004 | c0004 | t0004 | g0013 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03139 | hp2 | a0004 | c0004 | t0004 | g0013 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03209 | hp2 | a0003 | c0003 | t0003 | g0167 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03225 | hp2 | a0002 | c0002 | t0014 | g0232 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0208 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0024 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03453 | hp1 | a0003 | c0003 | t0003 | g0214 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03453 | hp2 | a0003 | c0003 | t0003 | g0185 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0233 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0204 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03516 | hp1 | a0002 | c0002 | t0016 | g0215 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03540 | hp1 | a0003 | c0003 | t0003 | g0181 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03579 | hp1 | a0003 | c0003 | t0003 | g0182 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03654 | hp1 | a0002 | c0002 | t0003 | g0231 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0156 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03704 | hp1 | a0001 | c0001 | t0010 | g0061 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03710 | hp1 | a0002 | c0002 | t0003 | g0157 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03831 | hp2 | a0001 | c0001 | t0009 | g0129 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03942 | hp2 | a0003 | c0003 | t0003 | g0035 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG04204 | hp1 | a0002 | c0002 | t0008 | g0206 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0228 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0162 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CHB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18906 | hp1 | a0003 | c0003 | t0003 | g0037 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18906 | hp2 | a0003 | c0003 | t0003 | g0036 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18949 | hp1 | a0002 | c0002 | t0003 | g0042 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18956 | hp2 | a0002 | c0002 | t0003 | g0213 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18960 | hp1 | a0002 | c0002 | t0012 | g0200 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18963 | hp2 | a0002 | c0002 | t0003 | g0041 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18970 | hp1 | a0005 | c0005 | t0002 | g0097 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19009 | hp2 | a0002 | c0002 | t0003 | g0042 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19030 | hp2 | a0003 | c0003 | t0003 | g0038 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19043 | hp1 | a0003 | c0003 | t0006 | g0155 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19043 | hp2 | a0004 | c0004 | t0004 | g0013 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19058 | hp2 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19077 | hp1 | a0008 | c0009 | t0003 | g0234 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19091 | hp2 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19240 | hp1 | a0002 | c0002 | t0011 | g0221 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ASW | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ASW | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA20805 | hp2 | a0003 | c0003 | t0003 | g0021 | EUR | TSI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA20905 | hp1 | a0003 | c0003 | t0003 | g0047 | SAS | GIH | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0207 | SAS | GIH | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0158 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02559 | hp1 | a0003 | c0003 | t0003 | g0184 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG02559 | hp2 | a0002 | c0002 | t0003 | g0040 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0046 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | USA | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
HG06807 | hp2 | a0003 | c0003 | t0003 | g0008 | AFR | USA | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA18955 | hp2 | a0002 | c0002 | t0003 | g0189 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | USA | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA20300 | hp2 | a0003 | c0003 | t0003 | g0037 | AFR | USA | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA21309 | hp1 | a0003 | c0003 | t0003 | g0008 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0003 | g0164 | REF | REF | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
homoSapiens_grch38 | hp1 | a0009 | c0006 | t0003 | g0123 | REF | REF | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:101281950
|
G | C | 7 | a0001a0002a0005others(4): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
missense_variant | MODERATE | c.1068C>G | p.Asp356Glu | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/7 | 1181/2953 | 1068/1203 | 356/400 | chr2 | 101281950 | ||
chr2:101295026
|
T | C | 1 | a0005 | 3 | HG01167.hp1 HG01169.hp1 NA18970.hp1 |
missense_variant | MODERATE | c.616A>G | p.Ile206Val | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/7 | 729/2953 | 616/1203 | 206/400 | chr2 | 101295026 | ||
chr2:101295168
|
T | C | 1 | a0010 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.474A>G | p.Ile158Met | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/7 | 587/2953 | 474/1203 | 158/400 | chr2 | 101295168 | ||
chr2:101308261
|
C | A | 1 | a0008 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.328G>T | p.Val110Phe | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | 441/2953 | 328/1203 | 110/400 | chr2 | 101308261 | ||
chr2:101308546
|
C | T | 1 | a0007 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.43G>A | p.Val15Met | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | 156/2953 | 43/1203 | 15/400 | chr2 | 101308546 | ||
chr2:101308552
|
G | A | 1 | a0004 | 4 | HG02258.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
missense_variant | MODERATE | c.37C>T | p.Arg13Cys | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | 150/2953 | 37/1203 | 13/400 | chr2 | 101308552 | ||
chr2:101308564
|
T | C | 6 | a0002a0003a0004others(3): Show | 192 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(189): Show |
missense_variant | MODERATE | c.25A>G | p.Ser9Gly | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | 138/2953 | 25/1203 | 9/400 | chr2 | 101308564 | ||
chr2:101308573
|
G | A | 1 | a0006 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.16C>T | p.Arg6Cys | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | 129/2953 | 16/1203 | 6/400 | chr2 | 101308573 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:101275643
|
G | A | 11 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(8): Show | 169 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1595C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1595 | chr2 | 101275643 | |||||
chr2:101275651
|
C | T | 4 | a0003c0003t0006a0003c0003t0013a0003c0003t0017others(1): Show | 9 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1587G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1587 | chr2 | 101275651 | |||||
chr2:101275652
|
G | A | 1 | a0001c0001t0007 | 2 | HG00621.hp2 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1586C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1586 | chr2 | 101275652 | |||||
chr2:101275670
|
T | C | 1 | a0002c0002t0011 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1568A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1568 | chr2 | 101275670 | |||||
chr2:101275676
|
C | T | 5 | a0001c0001t0002a0001c0001t0010a0002c0002t0002others(2): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1562G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1562 | chr2 | 101275676 | |||||
chr2:101275677
|
G | A | 1 | a0002c0002t0012 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1561C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1561 | chr2 | 101275677 | |||||
chr2:101275973
|
T | C | 4 | a0003c0003t0006a0003c0003t0013a0003c0003t0017others(1): Show | 9 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1265A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1265 | chr2 | 101275973 | |||||
chr2:101276033
|
A | G | 1 | a0002c0002t0014 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1205T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1205 | chr2 | 101276033 | |||||
chr2:101276172
|
C | T | 1 | a0001c0001t0010 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1066G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1066 | chr2 | 101276172 | |||||
chr2:101276544
|
T | C | 1 | a0002c0002t0014 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*694A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 694 | chr2 | 101276544 | |||||
chr2:101276573
|
AAAT | A | 1 | a0004c0004t0004 | 4 | HG02258.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*662_*664delATT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 662 | chr2 | 101276573 | |||||
chr2:101276778
|
A | T | 3 | a0003c0003t0006a0003c0003t0017a0004c0004t0004 | 8 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*460T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 460 | chr2 | 101276778 | |||||
chr2:101276895
|
A | T | 1 | a0001c0001t0009 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*343T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 343 | chr2 | 101276895 | |||||
chr2:101277064
|
A | G | 1 | a0001c0001t0005 | 3 | HG00099.hp1 HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*174T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 174 | chr2 | 101277064 | |||||
chr2:101277120
|
T | C | 1 | a0002c0002t0015 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*118A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 118 | chr2 | 101277120 | |||||
chr2:101277187
|
C | G | 1 | a0002c0002t0008 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 51 | chr2 | 101277187 | |||||
chr2:101277221
|
T | A | 1 | a0002c0002t0016 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 17 | chr2 | 101277221 | |||||
chr2:101308664
|
G | A | 1 | a0003c0003t0017 | 1 | HG02818.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-76C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | chr2 | 101308664 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:101277399
|
T | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160-118A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101277399 | ||||||
chr2:101277504
|
TC | T | 25 | a0001c0001t0002g0009a0001c0001t0002g0017a0001c0001t0002g0018others(22): Show | 32 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1160-224delG | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101277504 | ||||||
chr2:101277680
|
C | T | 4 | a0001c0001t0002g0026a0001c0001t0002g0056a0001c0001t0002g0069others(1): Show | 5 | HG01261.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160-399G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101277680 | ||||||
chr2:101277760
|
C | T | 47 | a0001c0001t0001g0062a0002c0002t0001g0002a0002c0002t0001g0003others(44): Show | 103 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1160-479G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101277760 | ||||||
chr2:101277856
|
C | CG | 10 | a0001c0001t0002g0051a0001c0001t0002g0077a0001c0001t0002g0082others(7): Show | 10 | HG01175.hp1 HG01433.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160-576dupC | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101277856 | ||||||
chr2:101278051
|
C | CA | 22 | a0002c0002t0001g0002a0002c0002t0001g0010a0002c0002t0001g0011others(19): Show | 51 | HG00609.hp2 HG00639.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.1160-771dupT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278051 | ||||||
chr2:101278220
|
C | T | 1 | a0002c0002t0001g0217 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1160-939G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278220 | ||||||
chr2:101278311
|
C | G | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160-1030G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278311 | ||||||
chr2:101278358
|
A | G | 200 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(197): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1160-1077T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278358 | ||||||
chr2:101278509
|
A | G | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1160-1228T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278509 | ||||||
chr2:101278512
|
TAA | T | 6 | a0002c0002t0003g0046a0002c0002t0003g0156a0002c0002t0003g0157others(3): Show | 7 | HG01243.hp1 HG01358.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1160-1233_1160-123 others(6): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278512 | ||||||
chr2:101278568
|
G | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160-1287C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278568 | ||||||
chr2:101278575
|
T | C | 1 | a0001c0001t0002g0086 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1160-1294A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278575 | ||||||
chr2:101278911
|
G | A | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1160-1630C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278911 | ||||||
chr2:101278912
|
A | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160-1631T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278912 | ||||||
chr2:101279072
|
G | A | 4 | a0001c0001t0002g0027a0001c0001t0002g0058a0001c0001t0005g0031others(1): Show | 6 | HG00099.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160-1791C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101279072 | ||||||
chr2:101279183
|
C | T | 3 | a0001c0001t0002g0063a0001c0001t0002g0067a0001c0001t0002g0084 | 3 | NA18972.hp1 NA19083.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1160-1902G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101279183 | ||||||
chr2:101279515
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160-2234A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101279515 | ||||||
chr2:101279518
|
G | A | 2 | a0002c0002t0001g0196a0006c0010t0001g0235 | 2 | HG01496.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1160-2237C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101279518 | ||||||
chr2:101279670
|
C | T | 6 | a0002c0002t0003g0046a0002c0002t0003g0156a0002c0002t0003g0157others(3): Show | 7 | HG01243.hp1 HG01358.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1159+2189G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101279670 | ||||||
chr2:101280055
|
G | A | 1 | a0003c0003t0006g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1159+1804C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280055 | ||||||
chr2:101280082
|
G | A | 1 | a0001c0001t0002g0087 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1159+1777C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280082 | ||||||
chr2:101280123
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1159+1736G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280123 | ||||||
chr2:101280154
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1159+1705G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280154 | ||||||
chr2:101280176
|
A | AAATAATA others(14): Show |
1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1159+1662_1159+168 others(25): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280176 | ||||||
chr2:101280201
|
A | AATAATAA others(2): Show |
6 | a0001c0001t0002g0016a0001c0001t0002g0051a0001c0001t0002g0052others(3): Show | 8 | HG00140.hp1 HG01175.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1159+1657_1159+165 others(13): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280201 | ||||||
chr2:101280201
|
A | AATAATG | 80 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(77): Show | 128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1159+1657_1159+165 others(10): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280201 | ||||||
chr2:101280201
|
A | AATGATG | 5 | a0001c0001t0002g0055a0001c0001t0002g0071a0001c0001t0002g0081others(2): Show | 5 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1159+1652_1159+165 others(10): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280201 | ||||||
chr2:101280201
|
A | G | 6 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0133others(3): Show | 8 | HG00140.hp2 HG00735.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1159+1658T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280201 | ||||||
chr2:101280204
|
G | A | 1 | a0003c0003t0003g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1159+1655C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280204 | ||||||
chr2:101280402
|
C | T | 1 | a0002c0002t0001g0011 | 4 | NA18960.hp2 NA18989.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+1457G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280402 | ||||||
chr2:101280526
|
A | G | 1 | a0002c0002t0001g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1159+1333T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280526 | ||||||
chr2:101280580
|
C | T | 2 | a0003c0003t0003g0008a0003c0003t0003g0154 | 6 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1159+1279G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280580 | ||||||
chr2:101280833
|
A | G | 84 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(81): Show | 133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1159+1026T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280833 | ||||||
chr2:101280863
|
C | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(82): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1159+996G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280863 | ||||||
chr2:101280868
|
C | T | 1 | a0002c0002t0001g0203 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1159+991G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280868 | ||||||
chr2:101280869
|
A | C | 1 | a0002c0002t0001g0203 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1159+990T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280869 | ||||||
chr2:101280880
|
A | G | 1 | a0001c0001t0002g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1159+979T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280880 | ||||||
chr2:101280881
|
A | G | 8 | a0002c0002t0002g0162a0002c0002t0003g0046a0002c0002t0003g0156others(5): Show | 9 | HG01243.hp1 HG01358.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1159+978T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280881 | ||||||
chr2:101280945
|
G | A | 2 | a0003c0003t0003g0022a0003c0003t0003g0037 | 5 | HG02809.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1159+914C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280945 | ||||||
chr2:101280961
|
G | A | 1 | a0002c0002t0001g0203 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1159+898C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280961 | ||||||
chr2:101280962
|
A | G | 1 | a0002c0002t0001g0203 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1159+897T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280962 | ||||||
chr2:101281090
|
C | A | 1 | a0003c0003t0003g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1159+769G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281090 | ||||||
chr2:101281131
|
A | G | 1 | a0003c0003t0006g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1159+728T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281131 | ||||||
chr2:101281228
|
CTG | C | 49 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(46): Show | 62 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1159+629_1159+630d others(4): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281228 | ||||||
chr2:101281343
|
G | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1159+516C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281343 | ||||||
chr2:101281401
|
G | A | 1 | a0002c0002t0001g0207 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1159+458C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281401 | ||||||
chr2:101281409
|
C | T | 200 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(197): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1159+450G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281409 | ||||||
chr2:101281420
|
A | ATTTTTTC others(3): Show |
1 | a0002c0002t0001g0203 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1159+429_1159+438d others(12): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281420 | ||||||
chr2:101281489
|
CT | C | 5 | a0001c0001t0002g0027a0001c0001t0002g0058a0001c0001t0002g0068others(2): Show | 6 | HG02040.hp2 HG02965.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1159+369delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281489 | ||||||
chr2:101281511
|
T | A | 145 | a0001c0001t0001g0062a0001c0001t0001g0126a0001c0001t0001g0133others(142): Show | 261 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1159+348A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281511 | ||||||
chr2:101281511
|
T | TA | 56 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(53): Show | 70 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1159+347dupT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281511 | ||||||
chr2:101281625
|
T | G | 1 | a0003c0003t0003g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1159+234A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281625 | ||||||
chr2:101281683
|
T | C | 1 | a0003c0003t0003g0187 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1159+176A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281683 | ||||||
chr2:101281738
|
C | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1159+121G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281738 | ||||||
chr2:101281744
|
G | A | 1 | a0002c0002t0001g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1159+115C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281744 | ||||||
chr2:101281760
|
G | A | 49 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(46): Show | 62 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1159+99C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281760 | ||||||
chr2:101281775
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1159+84A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281775 | ||||||
chr2:101282079
|
AAAAACAT others(11): Show |
A | 5 | a0003c0003t0006g0155a0003c0003t0006g0190a0003c0003t0006g0191others(2): Show | 8 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-40_961-23delAA others(16): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282079 | ||||||
chr2:101282161
|
G | A | 1 | a0003c0003t0003g0047 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.961-104C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282161 | ||||||
chr2:101282162
|
T | C | 1 | a0003c0003t0003g0047 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.961-105A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282162 | ||||||
chr2:101282207
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.961-150A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282207 | ||||||
chr2:101282562
|
C | T | 2 | a0005c0005t0002g0095a0005c0005t0002g0114 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.961-505G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282562 | ||||||
chr2:101282668
|
T | C | 211 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(208): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.961-611A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282668 | ||||||
chr2:101282941
|
G | A | 1 | a0003c0003t0003g0022 | 3 | HG02809.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.961-884C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282941 | ||||||
chr2:101282952
|
T | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.961-895A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282952 | ||||||
chr2:101282969
|
A | G | 48 | a0001c0001t0001g0062a0002c0002t0001g0002a0002c0002t0001g0003others(45): Show | 104 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.961-912T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282969 | ||||||
chr2:101282981
|
C | G | 1 | a0002c0002t0001g0223 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.961-924G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282981 | ||||||
chr2:101282984
|
GC | G | 93 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.961-928delG | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282984 | ||||||
chr2:101283093
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.961-1036C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283093 | ||||||
chr2:101283218
|
T | G | 3 | a0001c0001t0002g0004a0001c0001t0002g0059a0001c0001t0002g0089 | 11 | HG00438.hp1 HG00639.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.961-1161A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283218 | ||||||
chr2:101283329
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.961-1272A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283329 | ||||||
chr2:101283391
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0058 | 3 | HG02040.hp2 NA18963.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.961-1334G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283391 | ||||||
chr2:101283417
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.961-1360G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283417 | ||||||
chr2:101283587
|
G | A | 6 | a0002c0002t0003g0046a0002c0002t0003g0156a0002c0002t0003g0157others(3): Show | 7 | HG01243.hp1 HG01358.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.961-1530C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283587 | ||||||
chr2:101283927
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0058a0001c0001t0002g0079 | 4 | HG00280.hp2 HG02040.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-1870G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283927 | ||||||
chr2:101284038
|
T | C | 215 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(212): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.961-1981A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284038 | ||||||
chr2:101284078
|
G | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.960+2003C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284078 | ||||||
chr2:101284148
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.960+1933A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284148 | ||||||
chr2:101284205
|
C | G | 1 | a0002c0002t0001g0173 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.960+1876G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284205 | ||||||
chr2:101284276
|
C | T | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.960+1805G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284276 | ||||||
chr2:101284350
|
C | T | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.960+1731G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284350 | ||||||
chr2:101284373
|
ATT | A | 2 | a0003c0003t0003g0008a0003c0003t0003g0154 | 6 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+1706_960+1707d others(4): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284373 | ||||||
chr2:101284535
|
C | T | 1 | a0003c0003t0003g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.960+1546G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284535 | ||||||
chr2:101284542
|
T | C | 93 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.960+1539A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284542 | ||||||
chr2:101284552
|
G | T | 2 | a0001c0001t0002g0009a0001c0001t0002g0068 | 5 | NA18957.hp1 NA18973.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+1529C>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284552 | ||||||
chr2:101284587
|
C | A | 93 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.960+1494G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284587 | ||||||
chr2:101284957
|
C | T | 1 | a0001c0001t0002g0150 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.960+1124G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284957 | ||||||
chr2:101285014
|
T | A | 1 | a0002c0002t0003g0231 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.960+1067A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285014 | ||||||
chr2:101285051
|
T | C | 2 | a0002c0002t0011g0221a0002c0002t0014g0232 | 2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.960+1030A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285051 | ||||||
chr2:101285150
|
A | G | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.960+931T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285150 | ||||||
chr2:101285358
|
G | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.960+723C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285358 | ||||||
chr2:101285411
|
T | C | 6 | a0002c0002t0003g0039a0002c0002t0003g0041a0002c0002t0003g0042others(3): Show | 9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.960+670A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285411 | ||||||
chr2:101285455
|
T | C | 1 | a0001c0001t0002g0034 | 2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.960+626A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285455 | ||||||
chr2:101285798
|
C | T | 200 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(197): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.960+283G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285798 | ||||||
chr2:101286065
|
C | T | 1 | a0002c0002t0003g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.960+16G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101286065 | ||||||
chr2:101286296
|
A | G | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.864-119T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101286296 | ||||||
chr2:101286409
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0058a0001c0001t0002g0079 | 4 | HG00280.hp2 HG02040.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.864-232G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101286409 | ||||||
chr2:101286823
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.864-646C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101286823 | ||||||
chr2:101286854
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.864-677A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101286854 | ||||||
chr2:101286925
|
T | C | 1 | a0003c0003t0003g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.864-748A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101286925 | ||||||
chr2:101287074
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(45): Show | 61 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.864-897G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287074 | ||||||
chr2:101287237
|
G | A | 1 | a0001c0001t0002g0110 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.864-1060C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287237 | ||||||
chr2:101287286
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.864-1109C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287286 | ||||||
chr2:101287631
|
A | T | 1 | a0001c0001t0002g0071 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.863+1342T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287631 | ||||||
chr2:101287645
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(45): Show | 61 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.863+1328G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287645 | ||||||
chr2:101287743
|
GA | G | 6 | a0002c0002t0003g0039a0002c0002t0003g0041a0002c0002t0003g0042others(3): Show | 9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.863+1229delT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287743 | ||||||
chr2:101287904
|
A | T | 2 | a0001c0001t0002g0073a0001c0001t0002g0078 | 2 | HG00099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.863+1069T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287904 | ||||||
chr2:101287944
|
T | C | 202 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(199): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.863+1029A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287944 | ||||||
chr2:101288058
|
C | A | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.863+915G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288058 | ||||||
chr2:101288058
|
C | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.863+915G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288058 | ||||||
chr2:101288230
|
CT | C | 123 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(120): Show | 206 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.863+742delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288230 | ||||||
chr2:101288230
|
CTT | C | 88 | a0001c0001t0001g0032a0001c0001t0001g0136a0001c0001t0001g0137others(85): Show | 142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.863+741_863+742del others(2): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288230 | ||||||
chr2:101288260
|
G | A | 1 | a0002c0002t0003g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.863+713C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288260 | ||||||
chr2:101288387
|
G | A | 1 | a0003c0003t0003g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.863+586C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288387 | ||||||
chr2:101288428
|
G | A | 1 | a0001c0001t0002g0110 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.863+545C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288428 | ||||||
chr2:101288446
|
C | A | 1 | a0001c0001t0002g0090 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.863+527G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288446 | ||||||
chr2:101288517
|
C | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.863+456G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288517 | ||||||
chr2:101288666
|
A | C | 1 | a0001c0001t0002g0072 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.863+307T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288666 | ||||||
chr2:101288825
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.863+148A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288825 | ||||||
chr2:101288933
|
C | G | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.863+40G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288933 | ||||||
chr2:101289084
|
C | T | 1 | a0002c0002t0003g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.781-29G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289084 | ||||||
chr2:101289100
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781-45A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289100 | ||||||
chr2:101289143
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0140a0001c0001t0001g0141 | 4 | HG02074.hp2 HG02523.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-88G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289143 | ||||||
chr2:101289233
|
C | T | 6 | a0002c0002t0003g0039a0002c0002t0003g0041a0002c0002t0003g0042others(3): Show | 9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.781-178G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289233 | ||||||
chr2:101289429
|
A | G | 1 | a0001c0001t0002g0091 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.781-374T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289429 | ||||||
chr2:101289490
|
G | A | 200 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(197): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.781-435C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289490 | ||||||
chr2:101289492
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.781-437C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289492 | ||||||
chr2:101289560
|
C | A | 1 | a0002c0002t0003g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.781-505G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289560 | ||||||
chr2:101289610
|
C | A | 1 | a0008c0009t0003g0234 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.781-555G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289610 | ||||||
chr2:101289703
|
G | A | 1 | a0002c0002t0001g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.781-648C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289703 | ||||||
chr2:101289707
|
CA | C | 6 | a0001c0001t0001g0119a0001c0001t0002g0066a0001c0001t0002g0070others(3): Show | 6 | HG03492.hp1 NA18946.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-653delT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289707 | ||||||
chr2:101289708
|
A | G | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.781-653T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289708 | ||||||
chr2:101289773
|
C | T | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.781-718G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289773 | ||||||
chr2:101290549
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0131 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.781-1494T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101290549 | ||||||
chr2:101290603
|
G | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781-1548C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101290603 | ||||||
chr2:101290840
|
G | A | 1 | a0002c0002t0003g0046 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.781-1785C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101290840 | ||||||
chr2:101290860
|
T | G | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781-1805A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101290860 | ||||||
chr2:101291213
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.781-2158G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291213 | ||||||
chr2:101291340
|
G | A | 6 | a0003c0003t0003g0035a0003c0003t0003g0038a0003c0003t0003g0178others(3): Show | 8 | HG01099.hp2 HG01255.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-2285C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291340 | ||||||
chr2:101291370
|
C | T | 1 | a0002c0002t0003g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.781-2315G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291370 | ||||||
chr2:101291382
|
C | CA | 4 | a0003c0003t0003g0036a0003c0003t0003g0167a0003c0003t0003g0168others(1): Show | 5 | HG02622.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-2328_781-2327i others(3): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291382 | ||||||
chr2:101291400
|
C | T | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.781-2345G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291400 | ||||||
chr2:101291450
|
A | AT | 6 | a0001c0001t0002g0055a0001c0001t0002g0071a0002c0002t0001g0203others(3): Show | 10 | HG00741.hp1 HG01255.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.781-2396dupA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291450 | ||||||
chr2:101291564
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.780+2450G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291564 | ||||||
chr2:101291991
|
G | A | 4 | a0001c0001t0002g0060a0001c0001t0002g0064a0001c0001t0002g0091others(1): Show | 4 | NA18612.hp2 NA18999.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+2023C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291991 | ||||||
chr2:101292090
|
T | C | 1 | a0010c0007t0001g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.780+1924A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292090 | ||||||
chr2:101292109
|
T | C | 1 | a0001c0001t0002g0149 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.780+1905A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292109 | ||||||
chr2:101292167
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1847A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292167 | ||||||
chr2:101292181
|
A | G | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1833T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292181 | ||||||
chr2:101292216
|
T | C | 1 | a0003c0003t0003g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.780+1798A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292216 | ||||||
chr2:101292416
|
T | TCAAAGAT others(211): Show |
1 | a0003c0003t0006g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.780+1597_780+1598i others(220): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292416 | ||||||
chr2:101292489
|
G | A | 6 | a0002c0002t0003g0039a0002c0002t0003g0041a0002c0002t0003g0042others(3): Show | 9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.780+1525C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292489 | ||||||
chr2:101292526
|
G | A | 1 | a0001c0001t0002g0020 | 3 | HG03710.hp2 NA18950.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.780+1488C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292526 | ||||||
chr2:101292562
|
G | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1452C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292562 | ||||||
chr2:101292658
|
C | T | 2 | a0001c0001t0002g0070a0002c0002t0014g0232 | 2 | HG03225.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.780+1356G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292658 | ||||||
chr2:101292683
|
G | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1331C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292683 | ||||||
chr2:101292691
|
G | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1323C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292691 | ||||||
chr2:101292840
|
C | T | 6 | a0002c0002t0003g0039a0002c0002t0003g0041a0002c0002t0003g0042others(3): Show | 9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.780+1174G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292840 | ||||||
chr2:101292897
|
A | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1117T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292897 | ||||||
chr2:101292972
|
CT | C | 83 | a0001c0001t0001g0130a0001c0001t0001g0137a0001c0001t0002g0001others(80): Show | 133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.780+1041delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292972 | ||||||
chr2:101293093
|
C | T | 1 | a0003c0003t0003g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.780+921G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293093 | ||||||
chr2:101293190
|
C | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+824G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293190 | ||||||
chr2:101293594
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.780+420A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293594 | ||||||
chr2:101293664
|
T | C | 3 | a0003c0003t0003g0008a0003c0003t0003g0154a0003c0003t0003g0214 | 7 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+350A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293664 | ||||||
chr2:101293773
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.780+241G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293773 | ||||||
chr2:101293908
|
C | T | 1 | a0002c0002t0001g0222 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.780+106G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293908 | ||||||
chr2:101293962
|
C | T | 1 | a0002c0002t0001g0202 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.780+52G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293962 | ||||||
chr2:101293992
|
A | G | 1 | a0002c0002t0003g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.780+22T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293992 | ||||||
chr2:101294113
|
G | A | 1 | a0003c0003t0003g0179 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.712-31C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294113 | ||||||
chr2:101294217
|
T | C | 1 | a0001c0001t0002g0149 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.712-135A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294217 | ||||||
chr2:101294244
|
C | A | 2 | a0003c0003t0003g0022a0003c0003t0003g0037 | 5 | HG02809.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-162G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294244 | ||||||
chr2:101294344
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0121 | 2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.712-262G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294344 | ||||||
chr2:101294466
|
G | A | 1 | a0003c0003t0003g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.712-384C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294466 | ||||||
chr2:101294533
|
C | T | 1 | a0004c0004t0004g0013 | 4 | HG02258.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+398G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294533 | ||||||
chr2:101294573
|
C | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.711+358G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294573 | ||||||
chr2:101294674
|
C | G | 1 | a0002c0002t0001g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.711+257G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294674 | ||||||
chr2:101294676
|
G | C | 1 | a0002c0002t0003g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.711+255C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294676 | ||||||
chr2:101294794
|
C | A | 1 | a0001c0001t0002g0100 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.711+137G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294794 | ||||||
chr2:101294830
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0094 | 4 | HG00280.hp1 HG00738.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+101C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294830 | ||||||
chr2:101294879
|
A | G | 5 | a0003c0003t0006g0155a0003c0003t0006g0190a0003c0003t0006g0191others(2): Show | 8 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.711+52T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294879 | ||||||
chr2:101294923
|
A | G | 93 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
splice_region_variant&intron_variant | LOW | c.711+8T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294923 | ||||||
chr2:101295189
|
A | G | 2 | a0002c0002t0001g0196a0006c0010t0001g0235 | 2 | HG01496.hp2 HG02602.hp1 |
splice_region_variant&intron_variant | LOW | c.461-8T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295189 | ||||||
chr2:101295230
|
C | A | 7 | a0003c0003t0003g0022a0003c0003t0003g0036a0003c0003t0003g0037others(4): Show | 11 | HG02572.hp1 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.461-49G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295230 | ||||||
chr2:101295381
|
C | T | 1 | a0001c0001t0002g0102 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.461-200G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295381 | ||||||
chr2:101295436
|
C | T | 2 | a0003c0003t0003g0008a0003c0003t0003g0154 | 6 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-255G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295436 | ||||||
chr2:101295552
|
T | C | 1 | a0003c0003t0003g0185 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.461-371A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295552 | ||||||
chr2:101295607
|
G | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-426C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295607 | ||||||
chr2:101295615
|
C | A | 1 | a0001c0001t0002g0115 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.461-434G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295615 | ||||||
chr2:101295615
|
C | T | 6 | a0002c0002t0003g0039a0002c0002t0003g0041a0002c0002t0003g0042others(3): Show | 9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.461-434G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295615 | ||||||
chr2:101295636
|
G | A | 1 | a0002c0002t0003g0040 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.461-455C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295636 | ||||||
chr2:101295639
|
C | A | 6 | a0002c0002t0003g0039a0002c0002t0003g0041a0002c0002t0003g0042others(3): Show | 9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.461-458G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295639 | ||||||
chr2:101295658
|
C | A | 43 | a0002c0002t0003g0039a0002c0002t0003g0040a0002c0002t0003g0041others(40): Show | 63 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(60): Show |
intron_variant | MODIFIER | c.461-477G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295658 | ||||||
chr2:101295660
|
C | CA | 6 | a0001c0001t0002g0096a0001c0001t0002g0152a0003c0003t0003g0168others(3): Show | 6 | HG01361.hp2 HG02622.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-480dupT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295660 | ||||||
chr2:101295670
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.461-489T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295670 | ||||||
chr2:101295969
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0130a0001c0001t0009g0129 | 4 | HG02015.hp1 HG02602.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-788G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295969 | ||||||
chr2:101296096
|
C | T | 1 | a0002c0002t0001g0163 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.461-915G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296096 | ||||||
chr2:101296120
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-939A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296120 | ||||||
chr2:101296278
|
A | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-1097T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296278 | ||||||
chr2:101296657
|
G | T | 5 | a0001c0001t0001g0062a0002c0002t0001g0043a0002c0002t0001g0171others(2): Show | 6 | HG00438.hp2 HG00544.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-1476C>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296657 | ||||||
chr2:101296659
|
C | T | 2 | a0001c0001t0002g0108a0001c0001t0002g0151 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.461-1478G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296659 | ||||||
chr2:101296850
|
A | T | 3 | a0003c0003t0003g0177a0003c0003t0003g0180a0003c0003t0003g0181 | 3 | HG01167.hp2 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.461-1669T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296850 | ||||||
chr2:101296859
|
T | A | 13 | a0002c0002t0003g0231a0003c0003t0003g0021a0003c0003t0003g0047others(10): Show | 16 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.461-1678A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296859 | ||||||
chr2:101297037
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.461-1856G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297037 | ||||||
chr2:101297081
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.461-1900G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297081 | ||||||
chr2:101297122
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.461-1941A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297122 | ||||||
chr2:101297288
|
A | G | 1 | a0002c0002t0003g0040 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.461-2107T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297288 | ||||||
chr2:101297291
|
A | T | 3 | a0002c0002t0001g0005a0002c0002t0001g0216a0002c0002t0016g0215 | 10 | HG01884.hp1 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.461-2110T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297291 | ||||||
chr2:101297488
|
C | T | 6 | a0002c0002t0003g0046a0002c0002t0003g0156a0002c0002t0003g0157others(3): Show | 7 | HG01243.hp1 HG01358.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.461-2307G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297488 | ||||||
chr2:101297547
|
T | TG | 93 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.461-2367dupC | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297547 | ||||||
chr2:101297592
|
C | G | 1 | a0001c0001t0002g0064 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.461-2411G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297592 | ||||||
chr2:101297758
|
A | G | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-2577T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297758 | ||||||
chr2:101297821
|
G | T | 1 | a0003c0003t0003g0166 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.461-2640C>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297821 | ||||||
chr2:101297825
|
C | T | 1 | a0001c0001t0002g0112 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.461-2644G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297825 | ||||||
chr2:101297846
|
C | T | 3 | a0002c0002t0001g0005a0002c0002t0001g0216a0002c0002t0016g0215 | 10 | HG01884.hp1 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.461-2665G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297846 | ||||||
chr2:101297951
|
T | C | 23 | a0002c0002t0001g0002a0002c0002t0001g0010a0002c0002t0001g0011others(20): Show | 52 | HG00609.hp2 HG00639.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.461-2770A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297951 | ||||||
chr2:101297969
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0121 | 2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.461-2788G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297969 | ||||||
chr2:101297984
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.461-2803C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297984 | ||||||
chr2:101298016
|
T | G | 3 | a0003c0003t0003g0178a0003c0003t0003g0186a0003c0003t0003g0187 | 3 | HG01099.hp2 HG01255.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.461-2835A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298016 | ||||||
chr2:101298312
|
C | G | 1 | a0002c0002t0001g0194 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.461-3131G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298312 | ||||||
chr2:101298373
|
T | A | 1 | a0003c0003t0017g0236 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.461-3192A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298373 | ||||||
chr2:101298509
|
G | A | 1 | a0005c0005t0002g0097 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.461-3328C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298509 | ||||||
chr2:101298516
|
G | A | 1 | a0001c0001t0002g0027 | 2 | HG02040.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.461-3335C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298516 | ||||||
chr2:101298560
|
G | A | 2 | a0001c0001t0002g0108a0001c0001t0002g0151 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.461-3379C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298560 | ||||||
chr2:101298685
|
G | A | 3 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100 | 3 | HG00673.hp1 HG02135.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.461-3504C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298685 | ||||||
chr2:101298701
|
A | G | 1 | a0006c0010t0001g0235 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.461-3520T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298701 | ||||||
chr2:101298852
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.461-3671G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298852 | ||||||
chr2:101298947
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-3766A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298947 | ||||||
chr2:101299047
|
C | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-3866G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299047 | ||||||
chr2:101299075
|
C | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-3894G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299075 | ||||||
chr2:101299086
|
T | C | 1 | a0002c0002t0001g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.461-3905A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299086 | ||||||
chr2:101299094
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.461-3913A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299094 | ||||||
chr2:101299142
|
C | T | 2 | a0002c0002t0001g0192a0002c0002t0001g0193 | 2 | HG01069.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.461-3961G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299142 | ||||||
chr2:101299161
|
C | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-3980G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299161 | ||||||
chr2:101299187
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.461-4006A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299187 | ||||||
chr2:101299288
|
T | G | 2 | a0001c0001t0002g0019a0001c0001t0002g0116 | 4 | HG02896.hp2 HG03041.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-4107A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299288 | ||||||
chr2:101299442
|
C | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-4261G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299442 | ||||||
chr2:101299580
|
GC | G | 1 | a0002c0002t0001g0012 | 4 | HG02622.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-4400delG | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299580 | ||||||
chr2:101299582
|
T | A | 1 | a0002c0002t0001g0012 | 4 | HG02622.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-4401A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299582 | ||||||
chr2:101299633
|
G | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-4452C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299633 | ||||||
chr2:101299645
|
C | T | 1 | a0002c0002t0003g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.461-4464G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299645 | ||||||
chr2:101299765
|
T | C | 26 | a0002c0002t0003g0231a0003c0003t0003g0021a0003c0003t0003g0022others(23): Show | 35 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.461-4584A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299765 | ||||||
chr2:101299834
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-4653A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299834 | ||||||
chr2:101299915
|
G | A | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.461-4734C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299915 | ||||||
chr2:101300206
|
G | A | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.461-5025C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300206 | ||||||
chr2:101300297
|
G | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-5116C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300297 | ||||||
chr2:101300326
|
C | G | 6 | a0002c0002t0003g0039a0002c0002t0003g0041a0002c0002t0003g0042others(3): Show | 9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.461-5145G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300326 | ||||||
chr2:101300371
|
T | C | 6 | a0002c0002t0003g0039a0002c0002t0003g0041a0002c0002t0003g0042others(3): Show | 9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.461-5190A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300371 | ||||||
chr2:101300402
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.461-5221G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300402 | ||||||
chr2:101300427
|
A | G | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-5246T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300427 | ||||||
chr2:101300620
|
C | T | 87 | a0001c0001t0001g0025a0001c0001t0002g0001a0001c0001t0002g0004others(84): Show | 137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.461-5439G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300620 | ||||||
chr2:101300725
|
G | A | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.461-5544C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300725 | ||||||
chr2:101300864
|
T | G | 1 | a0001c0001t0002g0101 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.461-5683A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300864 | ||||||
chr2:101300881
|
G | A | 1 | a0002c0002t0003g0040 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.461-5700C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300881 | ||||||
chr2:101300903
|
C | T | 139 | a0001c0001t0001g0025a0001c0001t0002g0001a0001c0001t0002g0004others(136): Show | 210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.461-5722G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300903 | ||||||
chr2:101300997
|
T | C | 88 | a0001c0001t0001g0025a0001c0001t0002g0001a0001c0001t0002g0004others(85): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.461-5816A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300997 | ||||||
chr2:101301049
|
G | A | 88 | a0001c0001t0001g0025a0001c0001t0002g0001a0001c0001t0002g0004others(85): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.461-5868C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301049 | ||||||
chr2:101301238
|
G | GT | 83 | a0001c0001t0001g0025a0001c0001t0002g0001a0001c0001t0002g0004others(80): Show | 133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.461-6058dupA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301238 | ||||||
chr2:101301331
|
A | AT | 5 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0002g0063others(2): Show | 6 | HG02559.hp2 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.461-6151dupA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301331 | ||||||
chr2:101301331
|
AT | A | 6 | a0002c0002t0011g0221a0003c0003t0006g0155a0003c0003t0006g0190others(3): Show | 9 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.461-6151delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301331 | ||||||
chr2:101301689
|
TTTTG | T | 30 | a0002c0002t0003g0231a0003c0003t0003g0008a0003c0003t0003g0021others(27): Show | 43 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.460+6436_460+6439d others(6): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301689 | ||||||
chr2:101301770
|
T | A | 1 | a0001c0001t0002g0107 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.460+6359A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301770 | ||||||
chr2:101301771
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.460+6358G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301771 | ||||||
chr2:101301771
|
C | G | 4 | a0003c0003t0003g0036a0003c0003t0003g0167a0003c0003t0003g0168others(1): Show | 5 | HG02622.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.460+6358G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301771 | ||||||
chr2:101301779
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.460+6350C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301779 | ||||||
chr2:101301823
|
C | T | 1 | a0002c0002t0016g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.460+6306G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301823 | ||||||
chr2:101302033
|
T | C | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.460+6096A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302033 | ||||||
chr2:101302116
|
C | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+6013G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302116 | ||||||
chr2:101302196
|
T | C | 1 | a0002c0002t0001g0219 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.460+5933A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302196 | ||||||
chr2:101302245
|
G | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+5884C>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302245 | ||||||
chr2:101302262
|
A | G | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+5867T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302262 | ||||||
chr2:101302340
|
A | G | 88 | a0001c0001t0001g0025a0001c0001t0002g0001a0001c0001t0002g0004others(85): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.460+5789T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302340 | ||||||
chr2:101302445
|
G | A | 4 | a0001c0001t0002g0108a0001c0001t0002g0151a0002c0002t0002g0162others(1): Show | 4 | HG02145.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.460+5684C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302445 | ||||||
chr2:101302489
|
T | C | 1 | a0002c0002t0011g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.460+5640A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302489 | ||||||
chr2:101302586
|
T | C | 1 | a0002c0002t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460+5543A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302586 | ||||||
chr2:101302630
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+5499A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302630 | ||||||
chr2:101302697
|
C | T | 1 | a0002c0002t0003g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.460+5432G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302697 | ||||||
chr2:101302912
|
C | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 6 | HG02074.hp2 HG02080.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.460+5217G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302912 | ||||||
chr2:101302941
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+5188A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302941 | ||||||
chr2:101302981
|
TA | T | 46 | a0001c0001t0001g0062a0001c0001t0001g0124a0002c0002t0001g0002others(43): Show | 105 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.460+5147delT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302981 | ||||||
chr2:101302981
|
TAA | T | 135 | a0001c0001t0001g0025a0001c0001t0002g0001a0001c0001t0002g0004others(132): Show | 206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.460+5146_460+5147d others(4): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302981 | ||||||
chr2:101303077
|
G | C | 38 | a0002c0002t0002g0162a0002c0002t0003g0046a0002c0002t0003g0156others(35): Show | 52 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.460+5052C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303077 | ||||||
chr2:101303261
|
A | G | 2 | a0001c0001t0002g0051a0001c0001t0002g0052 | 2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.460+4868T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303261 | ||||||
chr2:101303274
|
T | C | 2 | a0002c0002t0011g0221a0002c0002t0014g0232 | 2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.460+4855A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303274 | ||||||
chr2:101303281
|
AT | A | 141 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0032others(138): Show | 231 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(228): Show |
intron_variant | MODIFIER | c.460+4847delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303281 | ||||||
chr2:101303281
|
ATT | A | 88 | a0001c0001t0001g0025a0001c0001t0002g0001a0001c0001t0002g0004others(85): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.460+4846_460+4847d others(4): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303281 | ||||||
chr2:101303373
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.460+4756G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303373 | ||||||
chr2:101303430
|
A | C | 1 | a0001c0001t0001g0120 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.460+4699T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303430 | ||||||
chr2:101303602
|
T | A | 1 | a0003c0003t0003g0154 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.460+4527A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303602 | ||||||
chr2:101303643
|
C | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+4486G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303643 | ||||||
chr2:101303643
|
CATACCTC others(80): Show |
C | 1 | a0002c0002t0003g0213 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.460+4399_460+4485d others(89): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303643 | ||||||
chr2:101303708
|
C | A | 1 | a0001c0001t0002g0020 | 3 | HG03710.hp2 NA18950.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.460+4421G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303708 | ||||||
chr2:101303710
|
TATCAATA others(80): Show |
T | 1 | a0002c0002t0001g0188 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.460+4332_460+4418d others(89): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303710 | ||||||
chr2:101303815
|
C | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.460+4314G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303815 | ||||||
chr2:101303817
|
T | C | 87 | a0001c0001t0001g0025a0001c0001t0002g0001a0001c0001t0002g0004others(84): Show | 137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.460+4312A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303817 | ||||||
chr2:101303829
|
T | C | 30 | a0002c0002t0003g0231a0003c0003t0003g0008a0003c0003t0003g0021others(27): Show | 43 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.460+4300A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303829 | ||||||
chr2:101303895
|
C | A | 3 | a0002c0002t0001g0005a0002c0002t0001g0216a0002c0002t0016g0215 | 10 | HG01884.hp1 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.460+4234G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303895 | ||||||
chr2:101303906
|
T | C | 1 | a0001c0001t0002g0111 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.460+4223A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303906 | ||||||
chr2:101304175
|
T | C | 1 | a0001c0001t0002g0112 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.460+3954A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304175 | ||||||
chr2:101304265
|
C | G | 7 | a0003c0003t0003g0022a0003c0003t0003g0036a0003c0003t0003g0037others(4): Show | 11 | HG02572.hp1 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.460+3864G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304265 | ||||||
chr2:101304393
|
C | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+3736G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304393 | ||||||
chr2:101304511
|
C | T | 1 | a0001c0001t0010g0061 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.460+3618G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304511 | ||||||
chr2:101304622
|
T | C | 1 | a0002c0002t0001g0217 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.460+3507A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304622 | ||||||
chr2:101304630
|
A | T | 1 | a0002c0002t0003g0039 | 2 | NA19058.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.460+3499T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304630 | ||||||
chr2:101304835
|
A | AT | 9 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0007g0049others(6): Show | 12 | HG00642.hp2 HG01074.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.460+3293dupA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304835 | ||||||
chr2:101304835
|
AT | A | 138 | a0001c0001t0001g0025a0001c0001t0001g0062a0001c0001t0001g0145others(135): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.460+3293delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304835 | ||||||
chr2:101304835
|
ATT | A | 6 | a0001c0001t0002g0113a0001c0001t0002g0115a0001c0001t0002g0116others(3): Show | 6 | HG01167.hp1 HG01257.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.460+3292_460+3293d others(4): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304835 | ||||||
chr2:101304897
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.460+3232C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304897 | ||||||
chr2:101304966
|
G | C | 1 | a0001c0001t0002g0117 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.460+3163C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304966 | ||||||
chr2:101305098
|
T | C | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+3031A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305098 | ||||||
chr2:101305290
|
C | A | 1 | a0001c0001t0001g0033 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.460+2839G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305290 | ||||||
chr2:101305341
|
C | G | 1 | a0002c0002t0003g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.460+2788G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305341 | ||||||
chr2:101305701
|
G | A | 2 | a0002c0002t0001g0012a0002c0002t0011g0221 | 5 | HG02622.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.460+2428C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305701 | ||||||
chr2:101305708
|
T | G | 194 | a0001c0001t0001g0025a0001c0001t0001g0062a0001c0001t0002g0001others(191): Show | 326 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(323): Show |
intron_variant | MODIFIER | c.460+2421A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305708 | ||||||
chr2:101305722
|
G | A | 1 | a0002c0002t0001g0220 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.460+2407C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305722 | ||||||
chr2:101305725
|
G | A | 184 | a0001c0001t0001g0025a0001c0001t0001g0062a0001c0001t0002g0001others(181): Show | 315 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.460+2404C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305725 | ||||||
chr2:101305792
|
G | A | 2 | a0002c0002t0001g0012a0002c0002t0011g0221 | 5 | HG02622.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.460+2337C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305792 | ||||||
chr2:101305850
|
G | A | 7 | a0002c0002t0001g0006a0002c0002t0001g0045a0002c0002t0001g0222others(4): Show | 14 | NA18939.hp1 NA18950.hp1 NA18956.hp1 others(11): Show |
intron_variant | MODIFIER | c.460+2279C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305850 | ||||||
chr2:101305898
|
A | G | 87 | a0001c0001t0001g0025a0001c0001t0001g0062a0001c0001t0002g0001others(84): Show | 137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.460+2231T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305898 | ||||||
chr2:101306024
|
G | A | 6 | a0002c0002t0003g0046a0002c0002t0003g0156a0002c0002t0003g0157others(3): Show | 7 | HG01243.hp1 HG01358.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.460+2105C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306024 | ||||||
chr2:101306031
|
G | A | 1 | a0001c0001t0002g0150 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.460+2098C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306031 | ||||||
chr2:101306117
|
G | T | 2 | a0001c0001t0007g0049a0001c0001t0007g0050 | 2 | HG00621.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.460+2012C>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306117 | ||||||
chr2:101306234
|
C | G | 1 | a0002c0002t0003g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.460+1895G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306234 | ||||||
chr2:101306264
|
C | T | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+1865G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306264 | ||||||
chr2:101306265
|
G | A | 2 | a0002c0002t0014g0232a0003c0003t0003g0230 | 2 | HG03017.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.460+1864C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306265 | ||||||
chr2:101306311
|
T | C | 107 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(104): Show | 189 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(186): Show |
intron_variant | MODIFIER | c.460+1818A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306311 | ||||||
chr2:101306418
|
G | A | 2 | a0002c0002t0003g0231a0003c0003t0003g0047 | 3 | HG02698.hp2 HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.460+1711C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306418 | ||||||
chr2:101306461
|
G | A | 1 | a0002c0002t0014g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+1668C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306461 | ||||||
chr2:101306535
|
C | G | 1 | a0001c0001t0002g0048 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.460+1594G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306535 | ||||||
chr2:101306833
|
C | T | 1 | a0003c0003t0003g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.460+1296G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306833 | ||||||
chr2:101306840
|
T | G | 1 | a0001c0001t0002g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.460+1289A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306840 | ||||||
chr2:101306874
|
C | T | 3 | a0002c0002t0001g0010a0002c0002t0001g0158a0002c0002t0001g0159 | 6 | HG01123.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.460+1255G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306874 | ||||||
chr2:101307024
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.460+1105C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307024 | ||||||
chr2:101307234
|
G | A | 1 | a0001c0001t0002g0034 | 2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.460+895C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307234 | ||||||
chr2:101307356
|
A | C | 2 | a0002c0002t0003g0156a0002c0002t0003g0157 | 2 | HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.460+773T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307356 | ||||||
chr2:101307542
|
A | G | 110 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(107): Show | 192 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(189): Show |
intron_variant | MODIFIER | c.460+587T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307542 | ||||||
chr2:101307574
|
C | T | 1 | a0003c0003t0006g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.460+555G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307574 | ||||||
chr2:101307913
|
C | G | 2 | a0003c0003t0003g0008a0003c0003t0003g0154 | 6 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.460+216G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307913 | ||||||
chr2:101307914
|
G | A | 1 | a0002c0002t0003g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.460+215C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307914 |